Arch Packaging Instant Gel Hand Sanitizer
Product Images NDC 79847-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Arch Packaging Instant Gel Hand Sanitizer (NDC 79847-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Arch Packaging Technologies Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Untitled (79847 001 2)

Label for Arch Packaging INSTANT Gel HAND SANITIZER with 70% Ethyl Alcohol, 32 fl oz (946 mL) gel form. The label highlights moisturizing and vitamin E content. It includes the Drug Facts panel with active ingredient 70% ethanol, usage instructions, warnings, inactive ingredients, and manufacturer information from Arch Packaging Technologies LLC in St. Louis, MO.*

FDA Label Image

Untitled (79847 001)

Drug Facts label for Arch Packaging INSTANT Gel HAND SANITIZER with 70% ethanol as the active ingredient. It includes use instructions, warnings about flammability and safety, directions for proper use, storage information, and lists inactive ingredients such as carbopol, glycerin, fragrance, vitamin E, and others.*

FDA Label Image

Untitled (79847001 3)

Label for Arch Packaging INSTANT Gel Hand Sanitizer containing 70% Ethyl Alcohol in a 1 gallon (3.785 L) size. The label highlights use with moisturizers and vitamin E and shows warnings, directions, ingredients, and flammability caution. Manufactured by Arch Packaging Technologies in St. Louis, MO, USA.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.